Allele Registry

Canonical Allele Identifier: PA127899

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019839

ClinVar Variation:

18195

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu378Lys	CA127898 NM_000477.7:c.1132G>A